Overview of Acid Gas Injection Operations in Western

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OVERVIEW OF ACID-GAS INJECTION OPERATIONS IN WESTERN CANADA
Stefan Bachu1* and William D. Gunter2
1
Alberta Energy and Utilities Board, Edmonton, AB, T6B 2X3, Canada
2
Alberta Research Council, Edmonton, AB, Canada
ABSTRACT
Over 2.5 Mt CO2 and 2.0 Mt H2S have been injected into deep saline aquifers and depleted hydrocarbon reservoirs
at 48 sites in western Canada by the end of 2003, driven by the need to dispose of H2S produced with natural gas
from sour gas reservoirs. Injection of acid gas (CO2 and H2S) occurs over a wide range of aquifer and reservoir
characteristics, acid gas compositions, and operating conditions. These acid-gas injection operations are a
commercial scale analogue to CO2 geological storage and are representative of aquifers and reservoirs in continental
sedimentary basins that have undergone compaction and erosion, like those between the Rocky Mountains and the
Appalachians in North America, where CO2 injection and geological storage on a large scale is most likely to be
implemented in Canada and the United States.
INTRODUCTION
Since 1990, faced with the challenge of reducing atmospheric emissions of hydrogen sulphide (H2S) produced
from “sour” hydrocarbon pools, oil and gas producers in the Alberta Basin in western Canada have been turning to
disposal of acid gas (H2S and CO2, with minor traces of hydrocarbons) by injection into deep geological formations.
To date, 48 applications for injection of acid gas produced at 42 different gas plants have been approved in western
Canada, of which 41 were active at the end of 2003 (Figure 1). Most operations inject acid gas at a single site
(single well), but a few inject or have injected at several sites, such that in total there are 48 injection sites for 42
operations. One operation was not implemented and two were rescinded after a period of operation, either because
injection volumes reached the approved limit, or because the gas plant producing the acid gas was decommissioned.
At a third operation the site was rescinded because the injection volume reached the limit of the injection reservoir,
and it was replaced with injection into a deeper saline formation. At another operation, three different sites have
been successively suspended by the regulatory agency because of reservoir overpressuring, with injection currently
occurring into a deep saline formation.
Figure 1: Location and status at the end of 2003 of acid-gas injection operations in western Canada.
*
Corresponding author: E-mail: Stefan.Bachu@gov.ab.ca
At three operations the acid gas is dissolved in water prior to injection, and the resulting weak acidic solution
(“sour water”) is injected. At seven other sites, of which three have been rescinded, wet acid gas (i.e. acid gas with
free water present) is injected. Dry acid gas (i.e. with no free water present) is injected at all other sites. Except for
the cases of injection in solution, the acid gas is injected as a dense fluid (liquid or supercritical). The cumulative
injection rate for all acid gas injection sites in western Canada reached more than 1 Mt/yr in 2003, of which
approximately 480 kt is CO2 (Figure 2a). The cumulative volume of acid gas injected to the end of 2003 reached
more than 4.5 Mt, of which slightly more than half is CO2 (Figure 2b).
These acid-gas injection operations represent a commercial-scale analogue to geological storage of CO2. The
technology and experience developed in the engineering aspects of acid-gas injection operations (i.e. design,
materials, leakage prevention and safety) can be adopted for large-scale operations for CO2 geological storage. The
characteristics of these operations provide a wealth of information that can be used for the screening and
identification of future sites for geological sequestration and storage of CO2. With the advent of emission trading,
acid gas injection could become even more appealing to oil and gas producers [1].
Figure 2: Time evolution of cumulative (all operations) a) injection rate; and b) injected volumes, at the acid-gas
injection operations in western Canada, showing also the fraction of injected H2S and CO2.
LICENSING AND OPERATING PARAMETERS
Applications for acid gas disposal need to conform to the specific requirements that deal with applications for
conventional oil and gas reservoirs [e.g. 2]. The selection of an acid-gas injection site needs to address various
considerations that relate to: 1) proximity of the injection site to the sour oil or gas facility that is the source of acid
gas; 2) confinement of the injected gas; 3) effect of acid gas on the rock matrix; 4) protection of energy, mineral and
groundwater resources; 5) equity interests; and 6) wellbore integrity and public safety [3, 4]. The specific location is
based on a general assessment of the regional geology and hydrogeology, which is designed to evaluate the potential
for leakage. Knowledge of the geological setting and characteristics is critical to assess the integrity of the host
formation or reservoir, and the short- and long-term fate of the injected acid gas. Of particular importance are
potential migration pathways within the injection zone (the spread of the injected acid gas plumes in aquifers is
considered in detail in a companion paper [5]) and from the injection zone to other formations, shallow groundwater
and/or the surface. To avoid leakage through the caprock or through induced fractures, the maximum bottomhole
injection pressure is set by regulatory agencies at 90% of the fracturing pressure in the injection zone. More
recently, regulatory agencies are limiting the bottom hole injection pressure in the case of injection into depleted
hydrocarbon reservoirs to the initial reservoir pressure or even less.
Regulatory agencies license only the maximum H2S content of the injected acid gas, which varies between 5%
and 97% mole fraction. The rest comprises mostly CO2, with a few percent C+ gases for the balance. The actual
average composition of the injected acid gas varies from 83% H2S and 14% CO2 to 2%H2S and 95% CO2. The
maximum approved wellhead injection pressure varies between 3,750 and 19,000 kPa. Approved daily injection
rates vary between 2,000 and 900,000 m3/day. Maximum allowed injection volumes vary between 6x106 and
1,876x106 m3. Based on the estimated total injection volume and aquifer or reservoir capacity, the acid gas injection
sites are planned to operate for periods of 10 to 25 years. For some specific case histories, see [6].
FACILITIES
After separation of any gas liquids, the produced sour gas is passed through a contactor or absorber tower in a
one- or two-stage process where the sour gas typically comes in contact with an amine or amine derivative solution.
The water-saturated acid-gas stream leaves the regeneration unit at 35 to 70 kPa and must be cooled, then
compressed for deep injection. After the acid gas is separated, it is compressed, dehydrated, pipelined and injected
through a disposal well (Figure 3). These operations depend on the properties of the H2S and CO2 mixture, the two
gases having similar phase equilibria [7, 8, 9]. The critical points are T=31.1oC and P=7,380 kPa for CO2 and
T=100.2oC and P=8,963 kPa for H2S. The phase behaviour of the acid gas system is represented by a continuous
series of two-phase envelopes separating the liquid and gas phases (e.g. Figure 3). Both CO2 and H2S form hydrates
at temperatures up to 10oC for CO2 and more than 30oC for H2S, even if free water is not present [7, 9, 10], thus it is
desirable to operate above the hydrate-forming temperature. Maintaining temperatures above 35oC (Figure 3)
prevents compressor breakdown and plugging, as well as plugging of the pipeline and injection well. Acid gas
obtained after the removal of H2S and CO2 from the sour gas is usually saturated with water vapor in the range of 2
to 6%. The solubility of water in both H2S and CO2, hence in acid gas, decreases as pressure increases up to 3-8
MPa, depending on temperature, after which it dramatically increases. The solubility minimum reflects the pressure
at which the acid-gas mixture passes into the dense liquid phase, where the solubility of water increases substantially
with increasing pressure due to the molecular attraction between these polar compounds [11, 12]. This property is
used in naturally dewatering the acid gas by compressing the gas from about 100 kPa to around 8 to 10 MPa for
injection, thus reducing the water content to less than 0.5 mole% to avoid pipe and well corrosion [11, 12, 13].
Figure 3: Typical operating conditions for acid gas injection showing the compression and dehydration cycle,
transportation from the gas plant to the injection well, and injection, in relation to the acid gas phase and
hydrate forming conditions (after [14]).
Most of the compressor drivers are electric motors in Alberta, and natural-gas fuelled engines in British Columbia.
In Alberta, adding gas engines to an approved plant requires a thorough review of NOx emissions for the plant.
Also, the maintenance cost of electric motors is less than that of natural gas engines. Most installations require only
four stages of compression. Maximum compressor discharge injection pressures range from 2.8 MPa to 8.9 MPa.
Generally, the compressed acid gas is injected in a pressure-temperature range where the liquid phase is stable,
resulting in an appreciable head pressure being generated due to the height of column of this liquid in the wellbore,
thus lowering the required compressor discharge pressure. To avoid cavitation, the acid gas must not enter the twophase region during compression. While sour gas or sweet gas that is injected in cycling (natural gas storage)
schemes requires dehydration, many acid gas disposal schemes do not need to dehydrate the acid gas. By the 4th
stage in a cycle (Figure 3), compression at pressures between 3 and 5 MPa will tend to dewater the acid gas if there
are no hydrocarbon impurities present [10]. Further compressing the acid gas increases the solubility of water in the
acid gas, such that residual excess water dissolves into the acid gas, and more than counteracts the decrease in
solubility due to inter-stage cooling. In the majority of cases dehydration is supplied by the compression cycle and
only in a few cases tri-ethylene glycol, refrigeration or a desiccant is used.
Pipelines reflect the fact that most of the current acid gas disposal projects handle small rates, in that most of the
lines have a diameter of 60 mm (2 inch nominal). The line lengths in many instances are short, reflecting the fact
that operators have either drilled the disposal well near the plant, or are using a prior existing well adjacent to the
plant. The design stress levels, and especially the actual operating stress levels, are low, again reflecting the low
injection pressure levels. Most lines are made out of carbon steel, although many of the short lines are made out of
stainless steel. Emergency shutdown valves are installed at both ends of the disposal pipeline. The pipelines
connect the plant compressors to the injection wells, and range in length from 100 m to 20 km, with diameters
ranging from 48 to 168 mm and wall thickness from 3.2 to 11 mm.
The bottom hole pressure needed for injection is provided by the pressure at the wellhead and the hydrostatic
weight of the acid gas in the well, minus friction losses down hole and across perforations. The wellhead is
equipped with a pressure control valve that regulates pressure. Regulations require that all disposal wells be
equipped with downhole packers, to protect the casing strings. Casing depths range from 856 to 3,335 metres.
Casing diameter ranges from 114 to 244 mm, while the tubing diameter ranges from 60 to 244 mm. Many wells are
equipped with L-80 grade tubing, which is considerably stronger than would be required for the experienced
injection pressure levels. To protect the tubing against the possibility of internal corrosion, several operators have
elected to use internally coated tubing. If the gas is undersaturated in water content, corrosion is minimal in any
case. Subsurface safety valves have been installed in many tubing strings, as a safety measure in the unlikely case
of backflow of acid gas from the formation. Many tubing strings are equipped with premium threads, to avoid
potential tubing leaks. Overall, many precautions have been applied in well completions to ensure safe operations.
SUBSURFACE CHARACTERISTICS
Table 1 summarizes the characteristics of the geological media into which the acid gas is injected. In 29 cases
injection takes place in carbonate rocks and in 19 cases in siliciclastics. In most cases shales and shaly siliciclastics
constitute the overlying confining unit (top seal), but also tight limestones, evaporites and anhydrites are present.
Reservoir containment of the acid gases by geological trapping is discussed in more detail in [15]. Other trapping
types for acid gas are hydrodynamic traps formed by deep aquifers, discussed in [16], and mineral traps discussed by
[17] and [18]. The initial formation pressure is generally subhydrostatic with respect to freshwater, except for one
case, in the Foothills in northeastern British Columbia, where the injection reservoir was initially slightly overpressured. In the case of acid gas injection into depleted oil or gas reservoirs, the original reservoir pressure was
drawn down as a result of production, such that formation pressure at the start of acid gas injection was less than the
original formation pressure, sometimes significantly, reaching as low as 1170 kPa. In 10 cases the formation
pressure at start-up was below the critical pressure of CO2.
TABLE 1: CHARACTERISTICS OF THE AQUIFERS AND OIL OR GAS RESERVOIRS USED FOR ACID
GAS INJECTION IN WESTERN CANADA.
Characteristic
Average injection depth (m)
Formation thickness (m)
Net pay (m)
Porosity (%)
Permeability (mD)
Formation pressure (kPa)
Formation temperature (˚C)
Water salinity (mg/l)
Oil gravity (˚API)
Gas specific gravity
Minimum Value
824
4
2
4
1
5,915
26
19,740
16
0.573
Maximum Value
3432
276
100
30
4,250
35,860
110
341,430
68
1.121
In-situ phase and thermodynamic properties of the formation brines and acid gases are discussed in more detail in
[19]. For the case of acid gas being injected into depleted oil reservoirs, the oils are medium to very light (24˚ API
to 68˚API), and in one case the oil is heavy (16˚API). Acid gases generally have a lower minimum miscibility
pressure than conventional hydrocarbon gases, therefore, they can be used in enhanced oil recovery (EOR), as it was
done at one site [20]. Reservoir gases are generally light (specific gravity less than 0.75). Because acid gas is
generally heavier than these reservoir gases, it may also be considered for use in enhanced gas recovery. More
details about the subsurface characteristics of the acid-gas injection in western Canada can be found in [21].
CONCLUSIONS
By the end of 2003, approximately 2.5 Mt CO2 and 2.0 Mt H2S have been successfully injected into deep
hydrocarbon reservoirs and saline aquifers in western Canada. This experience shows that CO2 storage in geological
media is a technology that can successfully be expanded to and applied in large-scale operations that will reduce
CO2 emissions into the atmosphere from large CO2 point sources. The size of the operations approved to date in
western Canada is relatively small, with approved injection rates and volumes generally less than 0.1 million m3/d
and 1000 million m3, respectively. The technology and experience developed in the engineering aspects of acid-gas
injection operations (i.e. design, materials, leakage prevention and safety) can be easily adopted for large-scale
operations for CO2 geological storage, since a CO2 stream with no H2S is less corrosive and less hazardous. No
safety incidents have been reported in the 15 years since the first operation in the world started injecting acid gas
into a depleted reservoir on the outskirts of the city of Edmonton, Alberta. Given that H2S is more toxic and
corrosive than CO2, the success of these acid-gas injection operations indicate that the engineering technology for
CO2 geological storage is in a mature stage. The major issues that need addressing in the near future are the longterm containment of the injected gases in the subsurface, and the safety of large-scale operations.
REFERENCES
1.
Sikora, R., S. Wong, E. Wichert, M. McCulloch, and W.D. Gunter. 2004. Economic and emission accounting
for acid gas injection projects – An example from KeySpan Brazeau River, Alberta, Canada. In: Proceedings of
the 7th International Conference on Greenhouse Gas Control Technologies. Volume 1: Peer-Reviewed Papers
and Plenary Presentations, Vancouver, BC, September 5-9, 2004.
2. Alberta Energy and Utilities Board. 2000. Guide 65: Resources Applications for Conventional Oil and Gas
Reservoirs, Alberta Energy and Utilities Board, Calgary, AB, Canada 113-136. DOI, URL
<eub.gov.ab.ca/bbs/products/guides/g65.pdf>.
3. Keushing, H. 1995. Hydrogen sulphide – if you don’t like it, put it back. Journal of Canadian Petroleum
Technology, Vol. 34, No. 6: 18-20.
4. Longworth, H.L., G.C. Dunn, and M. Semchuk. 1996. Underground disposal of acid gas in Alberta, Canada:
regulatory concerns and case histories. SPE Paper 35584, In: Proceedings Gas Technology Symposium,
Calgary, AB, Canada, 28 April – 1 May 1996, SPE, Richardson, TX, USA, 181-192.
5. Bachu, S., J.M. Nordbotten, and M.A. Celia. 2004. Evaluation of the spread of acid gas plumes injected in deep
saline aquifers in western Canada as an analogue for CO2 injection in continental sedimentary basins. In:
Proceedings of the 7th International Conference on Greenhouse Gas Control Technologies. Volume 1: PeerReviewed Papers and Plenary Presentations, Vancouver, BC, September 5-9, 2004.
6. Bachu, S. and W.D. Gunter. 2004. Acid gas injection in the Alberta Basin, Canada: A CO2 storage experience.
In: Barnes, S.J. and R.H. Worden (eds.): Geological Storage of Carbon Dioxide: Reducing Greenhouse Gas
Emissions, Geological Society of London Special Publication, Bath, UK. In press.
7. Carroll, J.J. and D.W. Lui. 1997. Density, phase behavior keys to acid gas injection. Oil and Gas Journal, Vol.
95, No. 25: 63-72.
8. Ng, H-J., J.J. Carroll, and J.R. Maddocks. 1999. Impact of thermophysical properties research on acid-gas
injection process design. In: Proceedings of the 78th Gas Processors Association Annual Convention, Nashville,
TN, March 1-3, 1999, Tulsa, OK, USA, 114-120.
9. Carroll, J. J. 1998. Phase diagrams reveal acid-gas injection subtleties. Oil and Gas Journal, Vol. 96, No. 9: 9296.
10. Carroll, J. J. 1998. Acid gas injection encounters diverse H2S, water phase changes. Oil and Gas Journal, Vol.
96, No. 10: 57-59.
11. Jones, S.G., D.R. Rosa, and J.E. Johnson. 2004. Acid-gas injection design requires numerous considerations.
Oil and Gas Journal, Vol. 102, No. 10: 45-51
12. Wichert, E. and T. Royan. 1996. Sulfur disposal by acid gas injection, SPE Paper 35585, In: Proceedings of the
Gas Technology Symposium, Calgary, AB, Canada, 28 April – 1 May 1996, SPE, Richardson, TX, USA, 193200.
13. Wichert, E. and T. Royan, T. 1997. Acid gas injection eliminates sulfur recovery expense. Oil and Gas Journal,
Vol. 95, No. 17: 67-72.
14. Clark, M.A., W.Y. Syrek, W.D. Monnery, A.K.M. Jamaluddin, D.B. Bennion, F.B.Thomas, E. Wichert, A.E.
Reed, and D.J. Johnson. 1998. Designing an optimized injection strategy for acid gas disposal without
dehydration. In: Proceedings of the 77th Gas Processors Association Annual Convention, Dallas, TX, March 1618, 1998, Tulsa, OK, USA, 49-56.
15. Buschkuehle, B.E. 2004. Geological trapping of acid gas injected underground in western Canada. In:
Proceedings of the 7th International Conference on Greenhouse Gas Control Technologies. Vancouver, BC,
September 5-9, 2004.
16. Michael, K. and K. Haug. 2004. Hydrodynamic trapping of injected acid gas in western Canada. In:
Proceedings of the 7th International Conference on Greenhouse Gas Control Technologies. Vancouver, BC,
September 5-9, 2004.
17. Perkins, E.H. and B.E. Buschkuehle. 2004. Mineralogy and geochemical trapping of acid gas in the Edmonton
area of central Alberta, Canada. In: Proceedings of the 7th International Conference on Greenhouse Gas
Control Technologies. Volume 1: Peer-Reviewed Papers and Plenary Presentations, Vancouver, BC,
September 5-9, 2004..
18. Gunter, W.D., Allen Pratt, B.E. Buschkuehle, and E.H. Perkins. 2004. Acid gas injection in the Brazeau Nisku
Q carbonate reservoir: Geochemical reactions as a result of the injection of an H2S-CO2 waste stream. In:
Proceedings of the 7th International Conference on Greenhouse Gas Control Technologies. Volume 1: PeerReviewed Papers and Plenary Presentations, Vancouver, BC, September 5-9, 2004.
19. Bachu, S. and J.J. Carroll. 2004. In-situ phase and thermodynamic properties of resident brine and acid gases
(CO2 and H2S) injected in geological formations in western Canada. In: Proceedings of the 7th International
Conference on Greenhouse Gas Control Technologies. Volume 1: Peer-Reviewed Papers and Plenary
Presentations, Vancouver, BC, September 5-9, 2004.
20. Davison, R.J., A. Mayder, D. W. Hladiuk, and J. Jarrell. 1999. Zama acid gas disposal/miscible flood
implementation and results. Journal of Canadian Petroleum Technology, Vol. 38, No. 2: 45-54.
21. Bachu, S. and K. Haug. 2005. In-situ characteristics of acid-gas injection operations in the Alberta Basin,
western Canada: demonstration of CO2 geological storage. In: Benson, S.M. (ed.): The CO2 Capture and
Storage Project (CCP) for Carbon Dioxide Storage in Deep Geologic Formations for Climate Change
Mitigation, Vol. 2, Elsevier, London, UK. In press.
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